Neonatal death

Symptom Information:

Symptom ID: HPO:0003811
Synonyms:
Neonatal lethal [HPO:0003811]
Neonatal period death [Orphanet:53550]
Newborn death (event) [Orphanet:53550]
Newborn death [Orphanet:53550]
Stillbirth/neonatal death [Orphanet:53550]
Death neonatal [Orphanet:53550]
Death neonatal [MedDRA:10011912]
Death neonatal (NOS) [MedDRA:10011912]
Quality:
Cross references:
Orphanet:53550 "Stillbirth/neonatal death" [Orphanet:53550]
UMLS:C0410916 "Newborn death" [Orphanet:53550]
Is a (Direct Parents):
MedDRA Death and sudden death
HPO         Death
Orphanet Life expectancy shortened
Is a (Whole tree): HPO:
MedDRA:
General disorders and administration site conditions(MedDRA:10018065)
    Fatal outcomes(MedDRA:10053172)
       Death and sudden death(MedDRA:10011907)
          Neonatal death(HPO:0003811)
Database Frequency: 44 / 7739
Resource:

All diseases associated with this symptom:

Atelosteogenesis type I (Orphanet:1190)
Autosomal recessive polycystic kidney disease (Orphanet:731)
Boomerang dysplasia (Orphanet:1263)
Combined oxidative phosphorylation defect type 8 (Orphanet:319504)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Diabetic embryopathy (Orphanet:1926)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
EPIDERMOLYSIS BULLOSA WITH DIAPHRAGMATIC HERNIA (OMIM:226735)
Familial primary pulmonary hypoplasia (Orphanet:2257)
Fetal Gaucher disease (Orphanet:85212)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
GENITOURINARY TRACT ANOMALIES (OMIM:305690)
GRANULOMAS, CONGENITAL CEREBRAL (OMIM:306300)
Greenberg dysplasia (Orphanet:1426)
HERNIA, ANTERIOR DIAPHRAGMATIC (OMIM:306950)
Hypotonia with lactic acidemia and hyperammonemia (Orphanet:137908)
Lethal Larsen-like syndrome (Orphanet:2371)
Lethal acantholytic epidermolysis bullosa (Orphanet:158687)
Lethal arthrogryposis - anterior horn cell disease (Orphanet:53696)
Lethal chondrodysplasia, Seller type (Orphanet:1421)
Lethal congenital contracture syndrome type 1 (Orphanet:1486)
Lethal congenital contracture syndrome type 3 (Orphanet:137783)
Lethal faciocardiomelic dysplasia (Orphanet:1972)
Lethal infantile mitochondrial myopathy (Orphanet:254857)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
Lung agenesis - heart defect - thumb anomalies (Orphanet:1120)
MEDIUM CHAIN 3-KETOACYL-CoA THIOLASE DEFICIENCY (OMIM:602199)
Marden-Walker syndrome (Orphanet:2461)
Meckel syndrome, type 4 (OMIM:611134)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
NEUTROPENIA, LETHAL CONGENITAL, WITH EOSINOPHILIA (OMIM:257100)
Neonatal hemochromatosis (Orphanet:446)
Pallister-Hall syndrome (Orphanet:672)
Perinatal lethal hypophosphatasia (Orphanet:247623)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
Reticular dysgenesis (Orphanet:33355)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
THANATOPHORIC DYSPLASIA, GLASGOW VARIANT (OMIM:273680)
THANATOPHORIC DYSPLASIA, TYPE II (OMIM:187601)
Thanatophoric dysplasia type 1 (Orphanet:1860)
ULNAR AGENESIS AND ENDOCARDIAL FIBROELASTOSIS (OMIM:276822)
Ulbright-Hodes syndrome (Orphanet:3404)
VISCERAL STEATOSIS, CONGENITAL (OMIM:228100)
X-linked immunoneurologic disorder (Orphanet:2571)